Diseases that affect the eye, including photoreceptor degeneration,
diabetic retinopathy, and
glaucoma, affect 11.8 million people in the US, resulting in vision loss and
blindness. Loss of sight affects patient quality of life and puts an economic burden both on individuals and the greater healthcare system. Despite the urgent need for treatments, few effective options currently exist in the clinic. Here, we review research on promising neuroprotective strategies that promote neuronal survival with the potential to protect against vision loss and
retinal cell death. Due to the large number of neuroprotective strategies, we restricted our review to approaches that we had direct experience with in the laboratory. We focus on drugs that target survival pathways, including
bile acids like UDCA and
TUDCA,
steroid hormones like
progesterone,
therapies that target
retinal dopamine, and
neurotrophic factors. In addition, we review rehabilitative methods that increase endogenous repair mechanisms, including exercise and electrical stimulation
therapies. For each approach, we provide background on the neuroprotective strategy, including history of use in other diseases; describe potential mechanisms of action; review the body of research performed in the retina thus far, both in animals and in humans; and discuss considerations when translating each treatment to the clinic and to the retina, including which
therapies show the most promise for each
retinal disease. Despite the high incidence of
retinal diseases and the complexity of mechanisms involved, several promising neuroprotective treatments provide hope to prevent
blindness. We discuss attractive candidates here with the goal of furthering
retinal research in critical areas to rapidly translate neuroprotective strategies into the clinic.